Nichols A J, Hiley C R
J Pharm Pharmacol. 1985 Feb;37(2):110-5. doi: 10.1111/j.2042-7158.1985.tb05017.x.
The nature of the adrenoceptors and dopamine receptors mediating vascular responses in the in-situ blood perfused superior mesenteric arterial bed of the rat have been studied. alpha 1-Adrenoceptor agonists produced vasoconstriction but alpha 2-agonists had no significant effect on vascular resistance. The vasoconstrictor effects of noradrenaline were antagonized by low doses of prazosin (26 nmol kg-1 i.v.). Isoprenaline and salbutamol produced vasodilation when the vasculature was preconstricted with arginine vasopressin. The responses to isoprenaline were potently antagonized by propranolol (1.69 mumol kg-1 i.v.) and weakly but significantly reduced by practolol (3.75 mumol kg-1 i.v.) whereas the responses to salbutamol were unaffected by the same dose of practolol. After preconstriction of the vasculature and alpha-adrenoceptor blockade, dopamine and apomorphine produced dilator responses with both compounds producing the same maximal response and apomorphine being 1.8 times more potent than dopamine. The dopamine responses were present after the animals had been pithed and were resistant to spiperone (506 nmol kg-1 i.v.) but were antagonized by cis-alpha-flupenthixol (460 nmol kg-1 i.v.). These results suggest that this vascular bed possesses vasoconstrictor alpha 1- but not alpha 2-adrenoceptors, vasodilator beta 1- and beta 2-adrenoceptors and vasodilator dopamine receptors which appear similar to the D1-type found centrally.
研究了介导大鼠原位血液灌注肠系膜上动脉床血管反应的肾上腺素能受体和多巴胺受体的性质。α1肾上腺素能受体激动剂可引起血管收缩,但α2激动剂对血管阻力无显著影响。低剂量的哌唑嗪(26 nmol kg-1静脉注射)可拮抗去甲肾上腺素的血管收缩作用。当血管用精氨酸加压素预收缩时,异丙肾上腺素和沙丁胺醇可引起血管舒张。普萘洛尔(1.69 μmol kg-1静脉注射)可有效拮抗对异丙肾上腺素的反应,而醋氨心安(3.75 μmol kg-1静脉注射)可使反应轻微但显著降低,而相同剂量的醋氨心安对沙丁胺醇的反应无影响。在血管预收缩和α肾上腺素能受体阻断后,多巴胺和阿扑吗啡产生舒张反应,两种化合物产生相同的最大反应,且阿扑吗啡的效力比多巴胺强1.8倍。在动物脊髓横断后仍存在多巴胺反应,且对舒必利(506 nmol kg-1静脉注射)有抗性,但可被顺式α-氟哌噻吨(460 nmol kg-1静脉注射)拮抗。这些结果表明,该血管床具有血管收缩性α1肾上腺素能受体而非α2肾上腺素能受体、血管舒张性β1和β2肾上腺素能受体以及血管舒张性多巴胺受体,后者似乎与中枢发现的D1型相似。